PRO ADVANTAGE INSTANT HAND SANITIZER  - alcohol gel 
NDC National Distribution & Contracting, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Pro Advantage Instant Hand Sanitizer Gel

Pro Advantage Instant Hand Sanitizer Gel


Active Ingredients:

Alcohol 62%

Purpose

Antiseptic

Use

To help reduce bacteria on the hands that can potentially cause disease.

Warning:

• For External Use Only
• Flammable, keep away from fire or flame.

When using this product

• Avoid contact with eyes, if this occurs rinse thoroughly with water and contact a physician.

Ask a doctor before use if you have

• Deep wounds, animals bites or serious burns.

Stop use and ask a doctor if

• Condition persists.

Keep out of reach of children.

• If swallowed get medical help or contact a Poison Control Center right away.

Directions:

Apply a liberal amount to hands and rub hands thoroughly until dry. Do not rinse or wipe off gel.

Inactive Ingredients:

Water, Glycerin, Fragrance, Carbomer, Triethanolamine, DMDM Hydantoin

REF: P779118 NDC 43128-118-04

Made in China
www.ProAdvantagebyNDC.com

Manufactured for NDC, Inc.
407 New Sanford Road, La Vergne, TN 37086

Product Labels

Hand Sanitizer Gel Label

PRO ADVANTAGE INSTANT HAND SANITIZER  
alcohol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:43128-118
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 620 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
TROLAMINE (UNII: 9O3K93S3TK)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43128-118-04 1 in 1 PACKAGE
1 237 mL in 1 BOTTLE, PUMP
2 NDC:43128-118-05 296 mL in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 03/08/2013
Labeler - NDC National Distribution & Contracting, Inc. (009831413)

Revised: 4/2013
Document Id: 7ed9372a-1c18-4a52-b81f-49d052835e4e
Set id: b1c1c4ef-68a1-4c12-ade9-41fb90a61c6c
Version: 3
Effective Time: 20130424
 
NDC National Distribution & Contracting, Inc.